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Characterization and treatment of acid-base and renal defects due to urethral obstruction in cats.

In 23 cats, urinary obstruction of 24 to 48 hours' duration caused marked azotemia, hyperphosphatemia, hyperkalemia, and metabolic acidosis. The metabolic acidosis was a consistent finding and was severe in all cats (venous pH, 7.11 +/- 0.09). Serum sodium and chloride were normal. Glycosuria was found in 17 (74%) of the cats. There was no clear difference in blood pH, serum chemical values, or electrolyte concentrations between cats obstructed 24 hours and those obstructed 48 hours or longer. At a mean of 8.4 hours after relief of obstruction, acid-base status was corrected to normal, using fluid replacement and sodium bicarbonate therapy. Blood urea nitrogen serum creatinine, and serum inorganic phosphorus improved significantly (P less than 0.01) at a mean of 19.5 hours after treatment. Variation in azotemia after fluid replacement suggested variable decreases in glomerular filtration rate after relief of obstruction. Hypokalemia occasionally developed after relief of obstruction during the postobstructive diuresis. It was concluded that fluid and electrolyte therapy must be regulated in response to the postobstructive diuresis, to ensure proper medical management.

Acid-Base Imbalance↗

Variable expression of the congenital obstructive posterior urethral membrane.

OBJECTIVES: To assess the variability of membranous folds in the posterior urethra and their relationship to urethral obstruction. METHODS: Endoscopic video recordings of 19 boys with a membranous lesion in the posterior urethra were obtained over a 2.5-year period. Six had an endoscopy after a prenatal diagnosis of obstructive uropathy and 13 boys presented with either a urinary tract infection or hematuria. RESULTS: Young's type I and type III appearances were seen in all with an obstructive membrane, and those with a less obstructing membrane probably had incidental pathologic conditions. CONCLUSIONS: These observations support the thesis that the congenital attachment of the verumontanum to the anterior wall of the posterior urethra is the embryologic fore-runner to the congenital obstruction of the posterior urethra, and that there may be a variable degree of persistence of that attachment, which in some boys is not obstructive.

Child↗

Antenatal diagnosis and management of urinary abnormalities.

Although much time, effort, and money have been expended in the area of fetal surgery and even though considerable unfortunate media publicity has resulted, the actual clinical problem is not one of great magnitude. Currently all those interested in this area agree that consideration of any intrauterine manipulation or surgery should be reserved for a fetus who has bilateral involvement that is progressive, destructive, and associated with oligohydramnios. Except for rare instances, this eliminates all fetuses except those with some type of urethral obstruction. Significant urethral obstruction accounts for approximately 10 per cent of all patients who have a prenatal diagnosis of a urologic abnormality. Of this 10 per cent, some will not be progressive, some will not be destructive, some will not involve both kidneys, and some will not develop oligohydramnios. Some of these patients will be diagnosed early enough in pregnancy to allow termination of the pregnancy if the involvement is significant and if termination is acceptable to the family. Some will be diagnosed late enough in pregnancy so that if the lungs are mature or can be stimulated to mature, early delivery and postnatal management can be elected. Some will have other associated lethal anomalies that can be diagnosed and would preclude any consideration of intrauterine manipulation or therapy. Some will have irreversible renal failure. Occasionally, the mother may refuse any proposed intrauterine therapy. Thus we are probably considering, on a theoretic basis, well under 1 per cent of all fetuses who have a prenatal diagnosis of urologic abnormalities. There may be some unusual situations that justify intrauterine manipulation. One that we encountered involved a fetus with an abdominal mass so large that a cesarean section was deemed necessary (Figs. 12 and 13). Aspiration of the mass just before delivery was performed to allow a vaginal delivery. Another case involved a pregnant woman who developed severe toxemia. The fetus was found to have a solitary renal cyst. Repeated aspirations of the cyst resulted in resolution of the toxemia, which promptly recurred when fluid reaccumulated in the fetal renal cyst. Insertion of a double-universe catheter from the cyst into the amniotic cavity allowed completion of the pregnancy, with the delivery of an otherwise normal fetus without recurrence of the toxemia. A recent report on fetal surgery from the International Fetal Surgery Registry, coauthored by the strongest advocate of intrauterine intervention, reached these conclusions.(ABSTRACT TRUNCATED AT 400 WORDS)

Diagnostic Errors↗

Urethral calibre measurements on micturition cystourethrograms in adult males. Part two: Subvesical obstruction.

Urethral calibres were measured on six locations in 73 patients with obstruction of the bladder neck or prostatic urethra. The results indicate that the bladder outlet is compatible with normal micturition at calibres of 6 mm. or more and abnormally narrowed at 4 mm. or less. The very narrow overlapping area between the diameter values in normal and obstructed urethras makes MCU an accurate method of measurement the diagnosis of subvesical obstruction. More distal parts of the urethra although proven to be normal may appear on the roentgenograms as less distended than an abnormally narrowed bladder neck or prostatic urethra.

Adult↗

[Modification of the tissue thickness of the bladder in obstruction by urethral stenosis].

In experimental obstructed bladder by urethral stenosis, the trigone and the detrusor walls thicken in a very important but different way. The thickened mucosa and submucosa of the total bladder show oedema and hypertrophy of the connective fibro-elastic tissue. Related to the different axis of the pressure inside the bladder and the specific muscular architecture of both regions, the adventitial and muscular layers show no modification in the trigone but they become thinner in the detrusor.

Animals↗

[Hydroelectric shock wave in the treatment of complex urethra obstruction].

Twenty-one patients with traumatic complex urethral obstruction were treated by hydroelectric shock wave (HSW). In the 21 patients, anterior urethral stricture was noted in 3 and posterior urethral obstruction in 18. The length of obstruction was 0.5-6cm. 15 patients were cured by single hydroelectric shock wave, 3 by HSW and electric resection, 2 by HSW with open operation, and 1 failed. The follow-up of 19 patients for 3 to 43 months showed no recurrence of urethral obstruction. The classification of traumatic complex urethral obstruction and the points for attention during treatment of hydroelectric shock wave are discussed.

Adolescent↗

Fetal monolateral urinoma and neonatal renal function outcome in posterior urethral valves obstruction: the pop-off mechanism.

The "fetal urinoma" is a clinical and diagnostic entity due to urinary extravasation, early diagnosed in fetal and/or neonatal period. Both urinoma and urinary ascites, whose pathogenesis is not clear, are recognized associations of uterero-pelvic junction obstruction (UPJO) and neonatal posterior urethral valves (PUV) related with a protected fetal and neonatal renal function. Clinical and experimental studies have demonstrated that fetal urinary tract obstruction results in severe renal parenchymal injury. The so called "pop-off" valve mechanism has been advocated to justify the upper tract function preservation. Protective "pop-off" mechanisms, such as a unilateral reflux and dysplasia, urinary extravasation and congenital bladder diverticula are present in about 30% of patients with PUV. Their presence correlates with better overall long-term renal function. This mechanism has been justified as a sort of self derivation, to explain the renal function preservation in fetal and neonatal period. In the last two years we observed three cases of fetal monolateral urinoma, prenatally detected in fetuses with diagnosis of PUV. All three cases did well for that concerning renal function despite some current opinions suggesting the necessity of a bilateral urinary extravasation in order to preserve upper urinary tract function.

Female↗